| Literature DB >> 16853849 |
Melek S Baymak1, Kellie L Vercoe, Petr Zuman.
Abstract
Spectrophotometric and electroanalytical studies indicate that one of the formyl groups of terephthalaldehyde in aqueous solution is present in about 23% as a geminal diol. Stronger covalent hydration of CHO in terephthalaldehyde than in p-nitrobenzaldehyde is attributed to a strong resonance interaction between the two formyl groups.Entities:
Year: 2005 PMID： 16853849 DOI： 10.1021/jp054475u
Source DB: PubMed Journal: J Phys Chem B ISSN： 1520-5207 Impact factor: 2.991